RecallHawk
Class I Recall

Hippie Organics- French Beans, 1Lb, UPC 1588701137

Alpine Fresh, Inc.

Summary

The FDA issued a Class I for Hippie Organics- French Beans, 1Lb, UPC 1588701137 by Alpine Fresh, Inc.. Reason: Potential to be contaminated with Listeria monocytogenes. Firm notified FDA of positive result for Hippie Organics- Alpine Fresh French Bean Lot IM313.

Details

Source

Food Recall

External ID

F-1081-2022

Action Date

2022-06-01

Status

Terminated

Category

food

Product Description

Hippie Organics- French Beans, 1Lb, UPC 1588701137

Lot/Code Info: Lot IM313626 Sell by 4/16/22

Quantity Affected: 1874 cases/10 bags each

Reason for Recall

Potential to be contaminated with Listeria monocytogenes. Firm notified FDA of positive result for Hippie Organics- Alpine Fresh French Bean Lot IM313626

Distribution

Domestic distribution only.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-14

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Alpine Fresh, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Alpine Fresh, Inc. have FDA actions?

This is the only FDA action we have on record for Alpine Fresh, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1081-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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